510(k) K810112

SWR DISPOSABLE PREP RAZOR by G.D. Searle and Co. — Product Code KDC

K810112 is an FDA 510(k) premarket notification submitted by G.D. Searle and Co. for the device "SWR DISPOSABLE PREP RAZOR". The FDA issued a decision of Substantially Equivalent on February 4, 1981. The device falls under product code KDC (Instrument, Surgical, Disposable), a Class I device regulated under 21 CFR 878.4800. G.D. Searle and Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 4, 1981
Date Received
January 16, 1981
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Surgical, Disposable
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type